A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194031



Internal ID20761071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44861389..44883076hg38UCSC Ensembl
chr10:45356837..45378524hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3821688
hg1921688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448539
Supporting Variants
Samples
Known GenesTMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194031
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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